Karuna Therapeutics Reports First Quarter 2022 Financial Results and Provides General Business Update
Karuna Therapeutics (NASDAQ: KRTX) reported a net loss of
- Completion of enrollment in the Phase 3 EMERGENT-2 trial for schizophrenia.
- Upcoming topline data expected from EMERGENT-2 in Q3 2022 and EMERGENT-3 in Q1 2023.
- Strong cash position of
$443.2 million to fund operations for at least the next 12 months. - Initiation of Phase 3 program for psychosis in Alzheimer’s disease on track for mid-2022.
- Net loss increased to
$58.2 million , up from$30.5 million year-over-year. - R&D expenses rose to
$43.8 million , impacting financial stability.
Completed enrollment in the Phase 3 EMERGENT-2 trial evaluating KarXT for the treatment of schizophrenia in the second quarter of 2022
Topline data from the Phase 3 EMERGENT-2 and EMERGENT-3 trials expected in the third quarter of 2022 and in the first quarter of 2023, respectively
On track to initiate Phase 3 program evaluating KarXT for the treatment of psychosis in Alzheimer’s disease in mid-2022
Company to host webcast event highlighting KarXT clinical programs, with a primary focus on the Phase 3 program in psychosis in Alzheimer’s disease, in late-May
“We have made significant progress advancing our comprehensive late-stage clinical programs for KarXT, most notably with the completion of enrollment of our registrational Phase 3 EMERGENT-2 trial in schizophrenia in the second quarter,” said
“The growth of our organization, and the continued progression and expansion of our development efforts, as seen through our ongoing Phase 3 schizophrenia programs evaluating KarXT as a monotherapy and adjunctive therapy, as well as the planned initiation of our Phase 3 program in psychosis in Alzheimer’s disease mid-year, is a testament to our belief that KarXT has the potential to offer a new, potentially transformative therapy for people living with serious mental illness,”
Pipeline Updates
Karuna is advancing a pipeline of novel drug candidates for the treatment of various psychiatric and neurological conditions. The clinical pipeline is led by KarXT (xanomeline-trospium), an oral investigational antipsychotic with a novel mechanism of action mediated via muscarinic cholinergic receptors, that is currently being evaluated in ongoing and planned late-stage clinical trials as a potential treatment for schizophrenia and psychosis in Alzheimer’s disease.
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KarXT for the treatment of schizophrenia. The EMERGENT program, the clinical program evaluating KarXT for the treatment of schizophrenia, includes the completed positive Phase 2 EMERGENT-1 trial and the following ongoing Phase 3 trials:
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EMERGENT-2: A five-week inpatient trial evaluating the efficacy and safety of KarXT compared to placebo in 246 adults with schizophrenia in the
U.S. - The Company completed enrollment of EMERGENT-2 in the second quarter of 2022, and anticipates topline data in the third quarter of 2022.
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EMERGENT-3: A five-week inpatient trial evaluating the efficacy and safety of KarXT compared to placebo in 246 adults with schizophrenia in the
U.S. andUkraine .-
The Company anticipates topline data in the first quarter of 2023. The company continues to enroll patients at clinical trial sites in the
U.S. , and is not enrolling patients at clinical trial sites in theUkraine at this time due to theUkraine -Russia conflict.
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The Company anticipates topline data in the first quarter of 2023. The company continues to enroll patients at clinical trial sites in the
- EMERGENT-4: A 52-week outpatient, open-label extension trial evaluating the long-term safety and tolerability of KarXT in adults with schizophrenia who completed EMERGENT-2 or EMERGENT-3.
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EMERGENT-5: A 52-week outpatient, open-label trial evaluating the long-term safety and tolerability of KarXT in adults with schizophrenia in the
U.S. andPuerto Rico who were not enrolled in EMERGENT-2 or EMERGENT-3.
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EMERGENT-2: A five-week inpatient trial evaluating the efficacy and safety of KarXT compared to placebo in 246 adults with schizophrenia in the
- KarXT for the treatment of schizophrenia in adults who experience an inadequate response to current standard of care. The Phase 3 ARISE trial evaluating the safety and efficacy of KarXT compared to placebo as an adjunctive treatment for schizophrenia in adults who experience an inadequate response to current standard of care is enrolling.
- KarXT for the treatment of psychosis in Alzheimer’s disease. The Company remains on track to initiate the Phase 3 program evaluating KarXT for the treatment of psychosis in Alzheimer’s disease in mid-2022.
- Discovery and early-stage pipeline. The Company continues to advance its novel formulations of KarXT, earlier pipeline of muscarinic receptor targeted programs, and its artificial intelligence-based target agnostic drug discovery program for treating psychiatric and neurological conditions.
Business Updates
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The Company plans to host a webcast event highlighting KarXT clinical programs on
Wednesday, May 25, 2022 . The webcast event will highlight progress across the ongoing and planned KarXT clinical programs, with a primary focus on the planned Phase 3 program evaluating KarXT for the treatment of psychosis in Alzheimer’s disease.
Anticipated Upcoming Milestones
- Initiation of the Phase 3 program evaluating KarXT for the treatment of psychosis in Alzheimer’s disease (mid-2022)
- Topline data from the Phase 3 EMERGENT-2 trial (3Q 2022)
- Topline data from the Phase 3 EMERGENT-3 trial (1Q 2023)
First Quarter 2022 Financial Results
The Company reported a net loss of
Research and development expenses were
General and administrative expenses were
The Company ended the quarter with
About
Forward Looking Statements
This press release contains forward looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, including statements regarding our expectations about the timing of our ongoing and planned clinical trials and regulatory filings, our goals to develop and commercialize our product candidates, our liquidity and capital resources and other statements identified by words such as “could,” “expects,” “intends,” “may,” “plans,” “potential,” “should,” “will,” “would,” or similar expressions and the negatives of those terms. Forward looking statements are not promises or guarantees of future performance, and are subject to a variety of risks and uncertainties, many of which are beyond our control, and which could cause actual results to differ materially from those contemplated in such forward-looking statements. These factors include risks related to our limited operating history, our ability to obtain necessary funding, our ability to generate positive clinical trial results for our product candidates and other risks inherent in clinical development, the timing and scope of regulatory approvals, changes in laws and regulations to which we are subject, competitive pressures, our ability to identify additional product candidates, risks relating to business interruptions resulting from the coronavirus (COVID-19) pandemic, and other risks set forth under the heading “Risk Factors” of our Annual Report on Form 10-K for the year ended
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Unaudited Consolidated Statements of Operations |
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Three Months Ended |
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2022 |
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|
2021 |
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License revenue |
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$ |
- |
|
|
$ |
- |
|
Operating expenses: |
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|
|
|
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Research and development |
|
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43,806 |
|
|
|
20,186 |
|
General and administrative |
|
|
14,788 |
|
|
|
9,777 |
|
Total operating expenses |
|
|
58,594 |
|
|
|
29,963 |
|
Loss from operations |
|
|
(58,594 |
) |
|
|
(29,963 |
) |
Other income (loss), net: |
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|
|
|
|
|
||
Impairment loss on right-of-use assets |
|
|
— |
|
|
|
(677 |
) |
Interest income |
|
|
237 |
|
|
|
143 |
|
Sublease income |
|
|
139 |
|
|
|
— |
|
Total other income (loss), net |
|
|
376 |
|
|
|
(534 |
) |
Net loss before income taxes |
|
|
(58,218 |
) |
|
|
(30,497 |
) |
Income tax provision |
|
|
— |
|
|
|
— |
|
Net loss attributable to common stockholders |
|
$ |
(58,218 |
) |
|
$ |
(30,497 |
) |
Net loss per share, basic and diluted |
|
$ |
(1.95 |
) |
|
$ |
(1.10 |
) |
Weighted average common shares outstanding used in computing net loss per share, basic and diluted |
|
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29,805,961 |
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|
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27,786,538 |
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Unaudited Consolidated Balance Sheet Data |
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Cash, cash equivalents and investments |
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$ |
443,187 |
|
|
$ |
493,991 |
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Working capital |
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|
448,716 |
|
|
|
497,121 |
|
Total assets |
|
|
474,474 |
|
|
|
527,671 |
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Total stockholders’ equity |
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$ |
453,688 |
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|
$ |
502,026 |
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View source version on businesswire.com: https://www.businesswire.com/news/home/20220505005281/en/
Investors:
518-338-8990
asmith@karunatx.com
Media:
917-886-0247
lsneider@karunatx.com
Source:
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